王安杰

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:工业催化

办公地点:西部校区化工实验楼B321

联系方式:大连市高新区凌工路2号大连理工大学西部校区B321

电子邮箱:ajwang@dlut.edu.cn

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Hydrodesulfurization of dibenzothiophene catalyzed by Ni-Mo sulfides supported on a mixture of MCM-41 and HY zeolite

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论文类型:期刊论文

发表时间:2008-07-15

发表刊物:APPLIED CATALYSIS A-GENERAL

收录刊物:SCIE、EI

卷号:344

期号:1-2

页面范围:175-182

ISSN号:0926-860X

关键字:hydrodesulfurization; mixed support; MCM-41; HY zeolite; dibenzothiophene

摘要:High-performance hydrodesulfurization (HDS) catalysts were prepared by supporting Ni-Mo sulfides on a mixture of mesoporous MCM-41 and microporous HY zeolite. The mixed support was obtained either by physically mixing [MCM-41-HY(M)] or by overgrowing MCM-41 over HY zeolite particles [MCM-41 HY(C)]. Their HDS activities were tested in a trickle bed reactor at 280-340 degrees C, total pressure 5.0 MPa, H-2/feed ratio 1200 Nm(3) m(-3) and WHSV 27 h(-1), using a solution of 0.8 wt% DBT (dibenzothiophene) in decalin as the feed. A synergetic effect of the components in the mixed supports was observed on the supported Ni-Mo sulfides. NiMo/MCM-41-HY(M) exhibited both high HDS activity and hydrocracking activity, whereas NiMo/MCM-41-HY(C) showed a comparable HDS activity but a much lower hydrocracking activity. Moreover, the increase in HDS activity of either catalyst was accompanied by an enhancement in the hydrogenation pathway. The large difference between NiMo/MCM-41-HY(M) and NiMo/MCM-41-HY(C) in the hydrocracking activity may result from their different pore structures. (C) 2008 Elsevier B.V. All rights reserved.